Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan; Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama, Japan.
Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan; JSR-Keio University Medical and Chemical Innovation Center (JKiC), Tokyo, Japan.
J Allergy Clin Immunol Pract. 2021 Oct;9(10):3767-3780. doi: 10.1016/j.jaip.2021.05.045. Epub 2021 Jul 8.
X-linked inhibitor of apoptosis protein (XIAP) deficiency is an infrequent inborn error of immunity that is often associated with refractory inflammatory bowel disease (IBD). The natural course of XIAP deficiency is typically associated with poor prognosis, and hematopoietic cell transplantation (HCT) is the only curative treatment.
To study (1) the effect of HCT on patients with XIAP deficiency undergoing HCT, (2) the status of XIAP deficiency-associated IBD after HCT, and (3) the gut microbiota of XIAP deficiency-associated IBD before and after HCT.
A nationwide survey of patients with XIAP deficiency was conducted. A spreadsheet questionnaire was collected from the physicians. Feces samples collected from the patients before and after HCT and their healthy family members were analyzed.
Twenty-six patients with XIAP deficiency underwent HCT by the end of March 2020, and 22 patients (84.6%) survived. All the survivors underwent a fludarabine-based reduced-intensity condition regimen. Acute graft-versus-host disease was observed in 17 patients (65.4%). Nineteen patients experienced refractory IBD before undergoing HCT. IBD improved remarkably after HCT. After HCT, the colonoscopic and pathological symptoms were restored to normal, and the pediatric ulcerative colitis activity index improved significantly. Gut microbiota indicated dysbiosis before HCT; however, it was improved to resemble that of the healthy family members after HCT.
This study revealed that HCT has a favorable outcome for XIAP deficiency. HCT rescues gut inflammation and dysbiosis in patients with XIAP deficiency.
X 连锁凋亡抑制蛋白(XIAP)缺乏症是一种罕见的遗传性免疫缺陷病,常伴有难治性炎症性肠病(IBD)。XIAP 缺乏症的自然病程通常预后较差,造血细胞移植(HCT)是唯一的根治性治疗方法。
研究(1)HCT 对接受 HCT 的 XIAP 缺乏症患者的影响,(2)HCT 后 XIAP 缺乏症相关 IBD 的状态,以及(3)HCT 前后 XIAP 缺乏症相关 IBD 的肠道微生物群。
对 XIAP 缺乏症患者进行了一项全国性调查。从医生那里收集了电子表格问卷。分析了患者在 HCT 前后及其健康家庭成员的粪便样本。
截至 2020 年 3 月底,26 例 XIAP 缺乏症患者接受了 HCT,22 例(84.6%)存活。所有幸存者均接受了氟达拉滨为基础的低强度条件方案。17 例(65.4%)患者发生急性移植物抗宿主病。19 例患者在接受 HCT 前患有难治性 IBD。HCT 后 IBD 明显改善。HCT 后,结肠镜和病理症状恢复正常,小儿溃疡性结肠炎活动指数显著改善。HCT 前肠道微生物群存在失调;然而,HCT 后其改善为类似于健康家庭成员的状态。
本研究表明 HCT 对 XIAP 缺乏症有良好的疗效。HCT 可挽救 XIAP 缺乏症患者的肠道炎症和失调。